NCT07713030

Brief Summary

Prediabetics is a condition where blood sugar levels are normal but not yet high enough to be diagnosed as type 2 diabetes. This phase offers a crucial point for timely intervention to delay or prevent type 2 diabetes. The objective of the study will be to find the effects of high intensity interval and continuous endurance training on glycemic control, BMI, Vo2 Max, pulmonary function and physical activity among prediabetic patients. Study design will be randomized control trial. Total 80 participants will be enrolled in study. The data will be collected from faculty of Riphah International University, Lahore. The study will be completed within 8 months after approval of synopsis. A simple random sampling will be used to assign the groups; group A and group B. Group A will be assigned high intensity interval training and group B will be assigned to continuous training.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 8, 2026

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 20, 2026

Completed
12 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
Last Updated

July 20, 2026

Status Verified

July 1, 2026

Enrollment Period

3 months

First QC Date

June 8, 2026

Last Update Submit

July 17, 2026

Conditions

Keywords

BMIvo2 Maxglycemic controlPhysical ActivityHigh-Intensity Interval Training

Outcome Measures

Primary Outcomes (5)

  • fasting blood glucose

    Participants were instructed to fast overnight for 8 to 12 hours. FBG was measured using an automated glucose analyzer

    12 weeks

  • Forced Vital Capacity

    Spirometry using devices like a digital spirometry will be used. Forced Vital Capacity (FVC) will be measured in liters (L) using spirometry. FVC represents the maximum volume of air that can be forcefully exhaled after a maximal inspiration.

    12 weeks

  • Forced Expiratory Volume in One Second

    Forced Expiratory Volume in One Second (FEV₁) will be measured in liters (L) using spirometry. FEV₁ represents the volume of air exhaled during the first second of a forced expiratory maneuver.

    12 weeks

  • FEV₁/FVC ratio

    The FEV₁/FVC ratio will be expressed as a percentage (%) and calculated from spirometric measurements to assess the degree of airflow limitation.

    12 weeks

  • HbA1c

    HbA1c was assesed through high performance liquid chromatography

    12 weeks

Secondary Outcomes (3)

  • Body mass index (BMI)

    12 weeks

  • IPAQ (short form) questionnaire

    12 weeks

  • Maximal Oxygen Uptake (VO₂max)

    12 weeks

Study Arms (2)

High-Intensity Interval Training

ACTIVE COMPARATOR

High intensity interval training is a training method that involves repeated bouts of short duration, highintensity exercise typicallyb performed at ≥ 85 -95% of maximal heart rate or vo2 max interspersed with period of low intensity recovery or complete rest.

Behavioral: High-Intensity Interval Training

Continuous Endurance Training

ACTIVE COMPARATOR

Continuous endurance training also called moderate intensity continuous training involves sustained exercise at a moderate and steady intensity typically 60to 75% of vo2 max or maximal heart rate performed for a continuous duration without rest intervals

Behavioral: Continuous Endurance Training

Interventions

5 minutes warm up including walk * 30s fast stairs climbing * 60s slow walk down * Repeat 5 to 6 rounds * 5 minute stretching or slow walk (cool down)

High-Intensity Interval Training

5 to 10 minute walking (warm up ) * 25 to 30minutes at 60 to 70 %continuous training * Continuous walk for 15 to 20 minutes. * 5 to 10 minutes stretching (cool down)

Continuous Endurance Training

Eligibility Criteria

Age35 Years - 54 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Sedentary lifestyle (Individuals reporting minimal structured physical activity e.g., \<30 minutes of exercise per week) .
  • Stable Medical Condition (No history of significant cardiovascular events, uncontrolled hypertension, or other major comorbidities).
  • Stable Body Weight (Stable body weight with changes less than 3 kg in the past 6 months).

You may not qualify if:

  • uncontrolled hypertension
  • history of heart disease
  • myocardial infarction
  • stroke
  • Use of Specific Medications (Current use of insulin or other medications affecting glucose metabolism or exercise response)
  • Severe Obesity (Individuals with a BMI ≥ 40 kg/m)
  • High fasting blood glucose (Fasting blood glucose of \>100mg.dl-1)
  • Previous history of respiratory problems
  • Smoking

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rihpah international university Lahore campus

Lahore, Punjab Province, 40100, Pakistan

RECRUITING

MeSH Terms

Conditions

Prediabetic StateGlucose IntoleranceMotor Activity

Interventions

High-Intensity Interval Training

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesHyperglycemiaBehavior

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Arjumand Bano, MS

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Muhammad Iqbal Tariq, Phd

CONTACT

Misdaq Batool, MS PT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 8, 2026

First Posted

July 20, 2026

Study Start

May 1, 2026

Primary Completion

August 1, 2026

Study Completion

August 1, 2026

Last Updated

July 20, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Locations